Canonical Allele Identifier: CA1515637601
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434421G= , CM000666.2:g.177434421G= GRCh38
NC_000004.11:g.178355575G= , CM000666.1:g.178355575G= GRCh37
NC_000004.10:g.178592569G= NCBI36
NG_011845.2:g.13083C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.767C= MANE Select ENSP00000264595.2:p.Ala256=
ENST00000264595.6:c.767C= ENSP00000264595.2:p.Ala256=
ENST00000502310.5:c.338C= ENSP00000423798.1:p.Ala113=
ENST00000506853.5:n.725C=
NM_000027.3:c.767C= NP_000018.2:p.Ala256=
NM_001171988.1:c.737C= NP_001165459.1:p.Ala246=
NR_033655.1:n.819C=
XM_006714123.2:c.*61C= XP_006714186.1:n.*61C=
XR_001741155.2:n.839C=
NM_000027.4:c.767C= MANE Select NP_000018.2:p.Ala256=
NM_001171988.2:c.737C= NP_001165459.1:p.Ala246=
NR_033655.2:n.753C=